Apparatus and method for autologous normovolemic hemodilution

ABSTRACT

A system and method for autologous normovolemic hemodilution (ANH) are disclosed. The system can include a vacuum canister, which is sized to accept donor bags of a predetermined capacity. The vacuum canister is connected to a vacuum source which applies a suction to the donor bag within the canister. The system can include a canister having a self-generated vacuum, which includes compressible sidewalls that are spring-loaded to provide negative pressure needed to collect blood from a patient without the use of a gravity-induced siphon gradient. Also disclosed are ANH systems and kits that rely on a gravity-induced siphon gradient for blood collection.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.11/318,286, now U.S. Pat. No. ______, filed Dec. 23, 2005, which claimspriority under 35 U.S.C. §119 of U.S. Provisional Application No.60/639,246, filed Dec. 27, 2004, the entire disclosure of which isincorporated herein by reference.

TECHNICAL FIELD

The present invention relates generally to the field of blood collectionand transfusion and, more particularly, to an apparatus and method forautologous normovolemic hemodilution.

BACKGROUND

Autologous blood transfusions, which are defined as the reinfusion ofthe patient's own blood, continue to be used in surgical settings. Onetype of autologous blood transfusion involves preoperative donation andstorage of a patient's blood. In such a process, a patient's blood iscollected, typically over a period of weeks or months, and stored fortransfusion at the time of surgery. While preoperative autologous blooddonation/transfusion is popular, the process suffers from somedrawbacks. These drawbacks can include limitations in the amount ofblood that can be collected over a period of time, wasting ofpre-donated blood because it is not needed or expired, and transfusionof the wrong blood due to clerical errors.

In response to these shortcomings, intraoperative hemodilution (alsoreferred to as autologous normovolemic hemodilution or ANH) has grown inpopularity. ANH includes the removal or collection of blood (typicallyjust before or at the start of a surgical procedure) with thesimultaneous infusion of appropriate cell-free solution(s) to maintainintravascular volume prior to surgical blood loss. The previouslycollected patient's blood is reinfused during or after surgery, asneeded, to maintain a desired post-ANH hemoglobin concentration.Typically, the anesthesiologist is responsible for the ANH procedure.ANH allows for collection and reinfusion of a greater volume of bloodthan preoperative autologous procedures because the patient is typicallysedated and often is on a ventilator. ANH reduces red blood cell lossbecause the blood lost during surgery has a lower hematocrit (thepercentage of whole blood that is comprised of red blood cells).

Conventional devices used for ANH typically include a standard blooddonation/transfer bag, e.g., a 500 cc bag, and rely on gravity for blooddrainage and collection. Such conventional transfer bag devices requirelong tubing to create the necessary siphon gradient for blood drainage.In order to accommodate the long tubing, the bags are often placed faraway from the patient making it more difficult to monitor the progressof the blood drainage. This can be problematic for several reasons. Theuse of long tubing increases the likelihood of clotting within thetubing. Having the bag out of sight increases the chances of collectingtoo much blood in a single bag, which could cause clotting, forgettingto agitate the bag periodically to mix the collected blood with ananticoagulant within the bag, and potentially knocking over the bag orpulling the line out of the bag and/or patient.

SUMMARY OF THE INVENTION

According to one aspect of the invention, there is provided anautologous normovolemic hemodilution (ANH) blood collection deviceincluding a canister that defines an internal volume for receiving ablood collection bag, the canister including a blood inlet port and avacuum inlet port. The canister is openable and provides a substantiallyair-tight seal around the blood collection bag.

According to another aspect of the present invention, there is providedan autologous normovolemic hemodilution (ANH) blood collection deviceincluding a canister having resilient, compressible sidewalls and acompression device operative to compress the canister. The resilientcanister sidewalls are operative to return to an decompressed statefollowing compression, thereby generating a negative pressure within thecanister of sufficient magnitude to draw blood from a patient.

According to another aspect of the invention, there is provided a devicefor collecting blood from a patient through a blood collection line, thedevice including a canister in fluid communication with the patient, thecanister being configured to self-generate an internal negative pressureof sufficient magnitude to draw blood from the patient.

Although various features are described and are illustrated inrespective drawings/embodiments, it will be appreciated that features ofa given drawing or embodiment may be used in one or more other drawingsor embodiments of the invention.

The foregoing and other features of the invention are hereinafter morefully described and particularly pointed out in the claims, thefollowing description setting forth in detail certain illustrativeembodiments of the invention, these being indicative, however, of but afew of the various ways in which the principles of the invention may beemployed.

BRIEF DESCRIPTION OF DRAWINGS

These and further features of the present invention will be apparentwith reference to the following description and drawings, wherein:

FIG. 1A and FIG. 1B are diagrammatic side view illustrations of anautologous normovolemic hemodilution (ANH) blood collection device andsystem in accordance with an exemplary embodiment of the presentinvention;

FIG. 2A and FIG. 2B are diagrammatic side view illustrations of an ANHblood collection device and system in accordance with another exemplaryembodiment of the invention;

FIG. 3 is a diagrammatic illustration of an ANH blood collection deviceshown in a compressed condition and a decompressed condition inaccordance with another exemplary embodiment of the present invention;

FIG. 4 is a diagrammatic illustration of an ANH blood collection device,kit and system in accordance with another exemplary embodiment of thepresent invention; and

FIG. 5 is a diagrammatic illustration of an ANH blood collection device,kit and system in accordance with another embodiment of the presentinvention.

FIGS. 6A-6C are diagrammatic side view illustrations of an ANH bloodcollection device usable in connection with the systems illustrated inFIG. 4 and FIG. 5.

DISCLOSURE OF INVENTION

In the detailed description that follows, corresponding components havebeen given the same reference numerals regardless of whether they areshown in different embodiments of the present invention. To illustratethe present invention in a clear and concise manner, the drawings maynot necessarily be to scale and certain features may be shown insomewhat schematic form.

An exemplary autologous normovolemic hemodilution (ANH) blood collectionsystem according to the present invention is indicated generally by thenumeral 10 in the accompanying drawings. Artisans will appreciate thatANH generally includes the removal or collection of a patient's blood(typically just before or at the start of a surgical procedure) with thesimultaneous infusion of appropriate cell-free solution(s) to maintainintravascular volume prior to or concurrent with surgical blood loss.The previously collected patient's blood is re-infused during or aftersurgery, as needed, to maintain the desired post-ANH hemoglobinconcentration. While the present invention is being described inconnection with ANH blood collection, it is to be appreciated that thepresent invention is applicable. Further, while the present invention isbeing described with reference to blood collection, it is to beappreciated that the present invention may find application inconjunction with other fluid collection without departing from the scopeof the present invention.

As described below with respect to exemplary embodiments, the ANH bloodcollection system 10 includes a blood collection device 12 (alsoreferred herein as a canister) that can collect or otherwise draw bloodfrom a patient 14 without the use of a gravity-induced siphon gradient.As is discussed more fully below, the blood collection device forcanister can be disposed at a vertical height that is at or above thevertical height of a “draw point” on a patient (e.g., the point on thepatient from which blood is drawn, such as the arm or leg).

With reference to FIG. 1A and FIG. 1B, an ANH blood collection system 10is provided. The system 10 includes a blood collection device 12 (alsoreferred to herein as a canister or a vacuum canister). The canister 12includes substantially rigid walls (e.g., sidewalls, a bottom wall, anda top wall or cover), which define an internal volume 16 within which adonor or collection bag 18 is received. The donor bag 18 can be aconventional donor bag, such as a standard 513 cc (cubic centimeters)bag. Typically, the donor bag 18 includes a predetermined amount ofanticoagulant (e.g., 63 cc) disposed therein to prevent or minimizeclotting of blood as it is collected within the bag. The canister 12includes or otherwise defines a blood inlet port 20 through which bloodis drawn from the patient 14 through flexible tubing 22 (also referredto as a draw line) into the collection bag 18 through the blood inletport 20. The blood inlet port 20 includes suitable sealing means 24,such as a rubber seal, a foam rubber seal, a gasket or the like. Thesealing means 24 facilitate a substantially air-tight seal that issuitable for supporting a vacuum of at least about −25 millimeters ofmercury (mm of Hg), for example.

The canister 12 further includes or otherwise defines a vacuum inletport 26, which sealably receives flexible tubing 28 that is connected toa vacuum source 30. As is discussed above with respect to the bloodinput port, the vacuum inlet port includes suitable sealing means 32.The vacuum source 30 can include any suitable vacuum source, such asthose commonly found in many hospital and operating rooms. The vacuumsource 30 evacuates the internal volume 16 of the canister 12 and pullsthe collection bag 18, disposed therein, apart, thereby creating anegative pressure for drawing blood from the patient 14. Optionally, thesystem can include a regulator, which can be integral to the vacuumsource 30 or disposed between the vacuum source 30 and the canister 12in communication with the vacuum line. The regulator serves to controlthe vacuum generated by the vacuum source, often including a break pointsetting for safety (e.g., to avoid an unduly high negative pressure thatcould collapse a patient's blood vessel).

The canister 12 can be made from a substantially transparent orsubstantially translucent material, such as sturdy plastic or otherpolymer that allows for viewing of the contents of the donor bag throughthe canister. Alternatively, the canister can be made of a relativelyopaque material. The canister can include graduated markings 34 (e.g.,volume indicating markings) on the outer portion. The markings aid auser in determining the volume of blood and anticoagulant within thecollection bag. As is discussed below, the canister can define aninternal volume having a variety of shapes or geometries.

The canister is openable and closeable, and can be closed using anysuitable closure mechanism, such as cooperative threaded portions, asnap-fit mechanism and the like. The canister, in a closedconfiguration, is sealed to support a suitable vacuum therein (e.g., avacuum sufficient to create a negative pressure of at least about −25 mmof Hg within the collection bag), while being openable for insertion andremoval of collection bags. In one embodiment (illustrated in FIGS. 1Aand 1B), the canister includes a top portion 36 that is removable forinsertion and removal of donor bags. Alternatively, the canisterincludes a clamshell design (illustrated, for example, in FIGS. 2A and2B) that opens along a hinge 38 into a pair of halves or portions. Sucha clamshell design can include a seal substantially around the perimeterof the canister so that the canister can support a vacuum sufficient topull the collection bag apart.

In one embodiment, the canister is formed such that the internal volumeclosely corresponds to the volume of a collection bag that is filled toa desired volume (e.g., approximately 513 cc). Such a design provides anadditional check to limit the filling of or otherwise to preventoverfilling of a collection bag (and therefore to avoid or minimizeclotting within the bag. The clamshell canister can include appropriatehinges 38 on or along one of its edges (e.g., its bottom edge).Optionally, the canister may be designed to provide or otherwise definean adjustable internal volume for closely receiving collection bags ofvarying volume.

In this exemplary embodiment, the ANH system eliminates the need for useof gravity to collect blood by way of a siphon gradient. Therefore, thecanister can be disposed at a vertical height that is approximately evenwith or above the vertical height of the draw point on the patient. Inaddition, the drawline 22 can be of a shorter length, thereby furtherreducing the potential for clotting during blood collection.

With reference now to FIG. 3, an ANH blood collection system 10 includesa blood collection device 12 that provides a self-generated vacuum(e.g., a negative pressure that is sufficient to draw blood from apatient 14 through a length of tubing 22 when the blood collectiondevice 12 is at a height that is (i) somewhat lower than the draw pointon the patient, (ii) at approximately the same vertical height as thedraw point on the patient, or (iii) somewhat vertically higher than thedraw point on the patient).

The blood collection device 12 includes sidewalls 40 that arecompressible or otherwise collapsible. For purposes of this discussion,FIG. 3 illustrates the device in a compressed state on the right of thefigure and in a decompressed state on the left of the figure. Thesidewalls 40 can be made of a flexible plastic or plastic-like material,and include a resilient spring-like coil member 42 integrally formedwith the sidewalls 40. The coil member can be made of plastic, a metalor another suitable material. The blood collection device 12 includes acompression device 44 (such as a compression knob or other device formechanically compressing the device), which can be attached to aninternal drive mechanism 46. If the collection device 12 is in andecompressed state (shown on the left of FIG. 3), the compression knobcan be turned or otherwise actuated to compress the sidewalls of thecollection device (as shown on the right of FIG. 3).

In one embodiment, the device 12 includes an agitator 48 that isconnected to a lower portion 50 of the drive mechanism 46. The device 12optionally includes a de-airing port 52, for example, a one-way valve,which releases air from the internal volume of the device 12 as thedevice is compressed. The drive mechanism for 46 includes a lowerportion 50 for and a cooperative upper portion 54. In one embodiment,the lower and upper portions 50, 54 are cooperative threaded portions,for example a female threaded portion 54 and a male threaded portion 50.Once the device 12 is in the compressed state, the internal volume ofthe collection device 12 has been substantially evacuated. Once thedevice is compressed and the draw line 22 is coupled to the blood inletport 20 and the patient 14, the coil member 42 of the sidewalls providesa force to decompress or otherwise expand the device 12, therebygenerating a negative pressure within the device to draw blood from thepatient into the internal volume of the collection device. As the devicedecompresses, the lower portion 50 of the drive mechanism 46 rotateswith respect to the upper portion 54, thereby activating the agitator,which is attached to the lower portion 50. This agitation aids inpreventing clotting of blood collected within the collection device. Thecollection device can be formed to collect a predetermined volume ofanticoagulant, which is predisposed within the device before collection,and collected blood (e.g., approximately 513 cc of blood andanticoagulant). In one embodiment, the internal portions (e.g., thesidewalls, the drive mechanism and the agitator) of the collectiondevice incorporate the use a biocompatible coating, for example,covalently bonded heparin or the like, to inhibit clotting or othercomplement activations.

The system 10 can include a pressure regulator 60, which is disposedalong the draw line 20 between the patient 14 and the collection device12. The regulator serves to adjust the vacuum pressure generated by thecollection device, for example, to prevent collapsing of a patient'sblood vessel due to an excessive negative pressure.

In this embodiment, an external vacuum source is not required, whicheliminates the need for vacuum tubing. In addition, as is mentionedabove, the collection device 12 can be disposed at approximately thesame or higher vertical height as compared to the drawpoint on thepatient. As shown in FIG. 3, the collection device can include a bloodreinfusion port 64 disposed adjacent the bottom portion of the device.The blood reinfusion port allows for relatively easy reinfusion ofcollected blood into the patient at the appropriate time. Optionally,the compression knob 44 can be used to apply additional positivepressure within the collection device to aid in blood reinfusion.

FIG. 4 and FIG. 5 illustrate exemplary embodiments of an ANH bloodcollection system 10 in accordance with aspects of the presentinvention. FIG. 4 illustrates a system in which a single collection bag18 can be filled at one time, while FIG. 5 illustrates a system in whichone or more collections bags 18 can be filled at one time. In each ofthe illustrated embodiments, the system includes tubing 70 (e.g., anarterial line) that extends from the draw point on the patient to afirst stopcock 72 or other fluid directing device. The stopcock includesa number of ports for directing fluid in different directions.Optionally, one port is connected to a transducer 74 or other pressuremonitoring device via tubing 76. The stopcock 72 can be positioned todirect blood to the pressure sensor 74 for periodic monitoring of apatient's blood pressure. The system can include a mechanism forcontinuous blood pressure monitoring (e.g., a dual lumen arterial line).

One port is connected to a draw line 78 via a luer connection 80. Thedraw line 78 can be connected to a collection bag 18 via an additionalluer connection 82. In the embodiment illustrated in FIG. 4, the drawline 78 includes a luer connection at both the distal 82 and proximal 80ends. The collection bag, which typically includes anticoagulanttherein, includes a transfer line 84 with a luer connection 82 toconnect to or otherwise mate with the luer connection on the proximalend of the draw line. Each luer connection can include, for example, astandard luer fitting, a luer-lock fitting or any threaded,substantially water-tight connector. The use of luer connectionsfacilitates fast removal and installation of collection bags, whileproviding a mechanically secure and substantially water-tight connectionbetween the collection bag and the draw line. It is to be appreciatedthat the portion of the system that is designated generally as 90 can bethought of as an ANH kit.

FIG. 5 illustrates an alternative embodiment in which one or morecollection bags 18 can be filled. This embodiment is similar to theembodiment described above and illustrated in FIG. 4. The draw line 78includes a luer connection 80 at its distal end, but it also includes astopcock 86 or other fluid directing device along with a luer connection82 at its proximal end. This additional stopcock facilitatessimultaneous filling of one or more collection bags. It is to beappreciated that the portion of the system that is designated generallyas 90 can be thought of as an ANH kit.

With reference now to FIGS. 6A-6C, a collection device 12 for use withan ANH blood collection system is provided. It is to be appreciated thatthe collection device 12 can be used in conjunction with the systemsillustrated in FIGS. 4 and 5. The collection device 12, which issuitable for use with a standard donor or collection bag 18, includes afree-standing support 100 (also referred to as a frame or stand). Thecollection bag 18 can be secured to the support 100 such that the baghangs without making contact with the ground or other support surface.In one embodiment, the support 100 includes a weighing device 110, suchas spring scale. In this embodiment, the collection bag is hooked orotherwise secured to the spring scale such that the spring scaleindicates the weight of the collection bag as blood is collected in thecollection bag. This feature allows the user to monitor the volume ofblood collected within the collection bag (based on the known density ofwhole blood and the amount of coagulant within the bag), therebyproviding a relative accurate reading of the volume of whole blood andanticoagulant within the collection bag. In an alternative embodiment,the support 100 can include a “limiting” stand (e.g., an expanding standsuch as an A-frame stand), that distends out a predetermined amount asto only allow a predetermined amount of fluid to be contained within thecollection bag instead of using a scale. In one embodiment, the support100 with scale 110 can include a stop, which prevents the bag fromfilling with fluid pass a certain predetermined volume.

Although, particular embodiments of the invention have been described indetail, it is understood that the invention is not limitedcorrespondingly in scope, but includes all changes, modifications, andequivalents coming within the spirit and terms of the claims appendedhereto. In addition, it is to be appreciated that features shown anddescribed with respect to a given embodiment may also be used inconjunction with other embodiments.

Although the invention has been shown and described with respect to acertain preferred embodiment or embodiments, it is obvious thatequivalent alterations and modifications will occur to others skilled inthe art upon the reading and understanding of this specification and theannexed drawings. In particular regard to the various functionsperformed by the above described elements (components, assemblies,devices, compositions, etc.), the terms (including a reference to a“means”) used to describe such elements are intended to correspond,unless otherwise indicated, to any element which performs the specifiedfunction of the described element (i.e., that is functionallyequivalent), even though not structurally equivalent to the disclosedstructure which performs the function in the herein illustratedexemplary embodiment or embodiments of the invention. In addition, whilea particular feature of the invention may have been described above withrespect to only one or more of several illustrated embodiments, suchfeature may be combined with one or more other features of the otherembodiments, as may be desired and advantageous for any given orparticular application.

1. An autologous normovolemic hemodilution (ANH) blood collection devicecomprising a canister that defines an internal volume for receiving ablood collection bag, the canister including a blood inlet port and avacuum inlet port; and wherein the canister is openable and provides asubstantially air-tight seal around the blood collection bag.
 2. Thedevice of claim 1, wherein the canister defines an internal volume thatlimits the volume of blood collected within the blood collection bag. 3.The device of claim 1, wherein the canister is configured to define aninternal volume having a size and shape substantially corresponding to ablood collection bag filled to a desired maximum volume.
 4. The deviceof claim 1, wherein the canister is hinged.
 5. The device of claim 1,wherein the canister is openable and provides a seal around the bloodcollection bag that is suitable for supporting a vacuum of at least −25millimeters of Mercury.
 6. The device of claim 1, wherein the canisteris substantially transparent or substantially translucent.
 7. The deviceof claim 6, wherein an outer surface of the canister includes aplurality of volume-indicating markings.
 8. A system for ANH bloodcollection comprising the device of claim 1, and a vacuum source insubstantially air-tight communication with the canister via tubing. 9.The system of claim 8, further comprising a blood collection linebetween a draw point on a patient and the blood input port on thedevice.
 10. The system of claim 8, wherein the vacuum source evacuatesthe internal volume of the canister, thereby generating a negativepressure within the collection bag of sufficient magnitude to draw bloodfrom the patient through the collection line.
 11. The system of claim10, wherein the blood collection device is disposed at a vertical heightthat is at least as high as the vertical height of a draw point on thepatient.
 12. An autologous normovolemic hemodilution (ANH) bloodcollection device comprising: a canister having resilient, compressiblesidewalls; a compression device operative to compress the canister; andwherein the resilient canister sidewalls are operative to return to andecompressed state following compression, thereby generating a negativepressure within the canister of sufficient magnitude to draw blood froma patient.
 13. The device of claim 12, wherein the sidewalls includeflexible outer wall members and an integral coil member.
 14. The deviceof claim 12, wherein the compression device is a rotatable compressionknob.
 15. The device of claim 12, further comprising an agitatorconnected to a drive mechanism within the canister.
 16. The device ofclaim 15, wherein the drive mechanism includes a lower portionthreadably engaging an upper portion, the upper portion being connectedto the compression knob.
 17. The device of claim 16, wherein the drivemechanism rotates as the canister returns to an uncompressed state, therotation rotating the agitator within the canister.
 18. The device ofclaim 16, wherein at least one of the internal portion of the sidewalls,the agitator and the drive mechanism are coated with an anticoagulant.19. The device of claim 12, wherein the canister includes a bloodreinfusion port and a blood input port.
 20. A system for ANH bloodcollection comprising the device of claim 19, a blood collection linebetween a draw point on a patient and the blood input port on thedevice.
 21. The system of claim 20, wherein the blood collection deviceis disposed at a vertical height that is at least as high as thevertical height of a draw point on the patient.
 22. The system of claim20, further comprising a pressure regulator disposed along the bloodcollection line in fluid communication with the patient and the bloodcollection device.
 23. A device for collecting blood from a patientthrough a blood collection line, the device comprising a canister influid communication with the patient, the canister being configured toself-generate an internal negative pressure of sufficient magnitude todraw blood from the patient.